TABLE 4.
Origin | Sample | Lineshape model | Component values | Component description | Reference |
---|---|---|---|---|---|
Human | Brain WM | Super‐Lorentzian |
T2,min,U = 5.48 μs T2,min,S = 102 μs δU = 1.07 ppm δS = 2.09 ppm |
U: Myelin S: Residual non‐aqueous content |
Current study |
Porcine | Brain WM | Super‐Lorentzian |
T2,min,U = 7.5 μs T2,min,S = 101 μs δU = 1.38 ppm δS = 1.91 ppm |
U: Myelin S: Residual non‐aqueous content |
Weiger et al. 13 |
Bovine | Myelin lipid extract | Super‐Lorentzian |
T2,min = 8 μs δ = 1.5 ppm |
Methylene, shortest and largest (74% of total myelin signal) | Wilhelm et al. 12 |
Ovine | Cervical spinal cord | Super‐Lorentzian | T2,min = 10 μs | Methylene frequency, shortest and largest | Seifert et al. 21 |
Bovine | Brain WM | Super‐Lorentzian (Gaussian‐based) |
σmin,U = 7.2 μs σmin,S = 87 μs δU = δS = 1.3 ppm |
U: Shortest and largest S: Remaining |
Manning et al. 27 |
Rat | Optic nerve | Lorentzian | T2 = 80 μs | Shortest and largest | Horch et al. 26 |
Note: Lorentzian‐based super‐Lorentzian components are characterized (in the time‐domain) by decay constant T2,min, while Gaussian‐based super‐Lorentzian components are characterized (in the time‐domain) by the SD of the narrowest (i.e., shortest) constituent Gaussian, σmin. In studies in which multiple values were provided for the same parameter, the mean value is given. δ denotes the component chemical shift, which was calibrated with water at 4.7 ppm.